STERISPINE LC CAGE

Intervertebral Fusion Device With Bone Graft, Lumbar

SAFE ORTHOPAEDICS

The following data is part of a premarket notification filed by Safe Orthopaedics with the FDA for Sterispine Lc Cage.

Pre-market Notification Details

Device IDK133893
510k NumberK133893
Device Name:STERISPINE LC CAGE
ClassificationIntervertebral Fusion Device With Bone Graft, Lumbar
Applicant SAFE ORTHOPAEDICS Parc Des Bellevues Allee R.Luxembourg-Bat Californie Eragny Sur Oise,  FR 95610
ContactPierre Dumouchel
CorrespondentPierre Dumouchel
SAFE ORTHOPAEDICS Parc Des Bellevues Allee R.Luxembourg-Bat Californie Eragny Sur Oise,  FR 95610
Product CodeMAX  
CFR Regulation Number888.3080 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeAbbreviated
3rd Party ReviewedNo
Combination ProductNo
Date Received2013-12-20
Decision Date2014-03-14
Summary:summary

NIH GUDID Devices

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